Related Experiment Video
Updated: Jun 3, 2026

Assessment of Mitochondrial Functions and Cell Viability in Renal Cells Overexpressing Protein Kinase C Isozymes
Published on: January 7, 2013
A tomato lycopene complex protects the kidney from cisplatin-induced injury via affecting oxidative stress as well as
Ayhan Dogukan1, Mehmet Tuzcu, Can Ali Agca
1Department of Nephrology, School of Medicine, Firat University, Elazig, Turkey.
Abstract:
Cisplatin-induced nephrotoxicity is related to an increase in oxidative stress in the kidney. Lycopene, a carotenoid found in tomatoes, is a potent dietary antioxidant. In the present study, we investigated the effect of the tomato lycopene complex against cisplatin-induced lipid peroxidation and nephrotoxicity in rats. Male Wistar rats (n = 28, 8 wk old, between 200-215 g) were divided into 4 groups: (a) control, (b) tomato lycopene complex (6 mg/kg, daily; consisting of 6% lycopene, 1.5% tocopherols, 1% phytoene and phytofluene, and 0.2% β-carotene), (c) cisplatin (7 mg/kg i.p., single dose), and (d) cisplatin + tomato lycopene complex. Cisplatin administration increased serum urea-N (171 vs. 37 mg/dl) and creatinine (1.80 vs. 0.42 mg/dl) and decreased body weight in comparison with the control rats (P < 0.001). Serum creatinine and urea-N levels were lower in rats treated with tomato lycopene complex + cisplatin compared with rats treated with cisplatin alone (P < 0.001). The renal tissue from the cisplatin-treated rats had greater malondialdehyde (MDA; 172 vs. 93 nmol/g) and 8-isoprostane levels (1810 vs. 610 pg/g) than that from the control rats (P < 0.001). Tomato lycopene complex prevented the rise of MDA and 8-isoprostane (P < 0.001). No measurable lycopene could be detected in the serum of the control and cisplatin-treated rats, whereas lycopene was observed in the serum of rats supplemented with tomato lycopene complex. Renal Bax protein expression was significantly higher in the cisplatin-treated rats than in the control rats, and tomato lycopene complex treatment significantly reduced Bax expression (P < 0.001). The expression of Bcl-2 was higher in tomato lycopene complex/cisplatin-treated rats than in the cisplatin-injected rats (P < 0.05). The expression of renal HSP60 and HSP70 was significantly lower in tomato lycopene complex + cisplatin-treated rats than in rats treated with cisplatin alone (P < 0.001). These results suggest that tomato lycopene complex has protective effects against cisplatin-induced nephrotoxicity and lipid peroxidation in rats.
Insights
Tomato lycopene complex protects against cisplatin-induced nephrotoxicity by reducing oxidative stress and lipid peroxidation in rats. This dietary antioxidant intervention improved kidney function markers and modulated key protein expressions, suggesting a therapeutic potential.
Area of Science:
- Biochemistry
- Toxicology
- Nutritional Science
Background:
- Cisplatin chemotherapy is associated with significant kidney damage, primarily due to increased oxidative stress.
- Lycopene, a potent antioxidant found in tomatoes, is being investigated for its potential protective effects against drug-induced toxicity.
Purpose of the Study:
- To investigate the protective effects of a tomato lycopene complex against cisplatin-induced nephrotoxicity and lipid peroxidation in a rat model.
- To evaluate the impact of tomato lycopene complex on oxidative stress markers and key protein expressions in cisplatin-treated rats.
Main Methods:
- Male Wistar rats were divided into four groups: control, tomato lycopene complex alone, cisplatin alone, and cisplatin plus tomato lycopene complex.
- Biochemical parameters (serum urea-N, creatinine), lipid peroxidation markers (MDA, 8-isoprostane), and protein expressions (Bax, Bcl-2, HSP60, HSP70) were analyzed.
- Lycopene levels in serum were measured to confirm supplementation.
Main Results:
- Cisplatin significantly increased serum urea-N and creatinine, decreased body weight, and elevated renal MDA and 8-isoprostane levels.
- Tomato lycopene complex administration significantly reduced these cisplatin-induced detrimental effects, including preventing the rise in MDA and 8-isoprostane.
- The complex also modulated the expression of apoptosis-related proteins (Bax, Bcl-2) and heat shock proteins (HSP60, HSP70), indicating reduced cellular damage.
Conclusions:
- Tomato lycopene complex demonstrates significant protective effects against cisplatin-induced nephrotoxicity and lipid peroxidation in rats.
- The findings suggest that lycopene's antioxidant properties contribute to mitigating cisplatin-induced kidney damage by reducing oxidative stress and influencing cell survival pathways.
Related Concept Videos
Electron Transport Chain: Complex I and II
ROS generation is regulated and maintained at moderate levels necessary...
The Intrinsic Apoptotic Pathway
Kidney Transplant II: Surgical Procedure
Acute Kidney Injury IV: Diagnostic Studies and Prevention
